MedPath

A Study of the Effects of Sitagliptin (MK0431) and Metformin on Incretin Hormone Concentrations (0431-050)(COMPLETED)

Phase 1
Completed
Conditions
Type 2 Diabetes
Interventions
Registration Number
NCT00975052
Lead Sponsor
Merck Sharp & Dohme LLC
Brief Summary

This study will determine the effect of concomitant administration of sitagliptin and metformin on post-meal incretin hormone concentrations in healthy adults.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
16
Inclusion Criteria
  • Subject is in good health
  • Subject has been a nonsmoker for at least 6 months
  • Subject is willing to avoid strenuous activity from the screening visit until the end of the study
  • Subject agrees not to consume grapefruit products during the study and to avoid all fruit juices 24 hours before and after study drug administration
Exclusion Criteria
  • Any history of stroke or neurological disorder
  • Subject has a history of cardiovascular, blood, endocrine or liver diseases
  • Subject has a history of cancer

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Asitagliptin phosphateSitagliptin alone
Primary Outcome Measures
NameTimeMethod
Weighted average active GLP-1 (glucagonlike peptide-1) concentrations4 hours after the postdose meal
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath